Skip to content

Motion Coaching Technology for Physical Therapy in Low Back Pain.

Validation of Motion Coaching Technology for Physical Therapy in Treating Patients With Chronic, Nonspecific Low Back Pain. A Pilot Project.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04411108
Enrollment
40
Registered
2020-06-02
Start date
2020-10-20
Completion date
2021-09-27
Last updated
2022-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain

Brief summary

In this study, we will compare exercise execution between two groups of patients: (1) individuals who undergo instruction session by a PT and then perform exercises with a written handout at home and (2) individuals who use the mHealth motion coach at home. Participants will perform the same 4 exercises. Both groups will be instructed to exercise at home, supported either by the handouts or the Motion Coach technology and then return after 1 week for assessment. For the assessment, standardized videos will be used to capture pose during exercise execution. Group 1 will perform the exercises with the written handout; group 2 will perform the exercises with the motion coach. Rating will be performed by a panel of PT professionals on the overall assessment of each exercises and on the three segments mentioned below that are exercise specific. The first group with PT instruction and written handout portion will be compared to the second group with the motion coach.

Interventions

OTHERKaia Back Pain App

The Kaia Back Pain App provides instructions on exercise execution to participants for one week

OTHERPhysiotherapist Exercise Instructions and written handouts

Participants will be instructed by physiotherapists in exercise execution and receive handouts and exercise for one week

Sponsors

Washington University School of Medicine
CollaboratorOTHER
Kaia Health Software
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
22 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age 22 - 65 * English speaking * Absence of neurologic deficits as assessed by the clinician, with 5/5 strength in all muscle groups in the lower extremities and no sensory deficits in the lower extremities * Pain located in the low back or posterior pelvic region * Self-reported mean pain score \>4 in the past 1 week as assessed by VAS pain score from 0-10 * Pain duration \>1 month to 5 years * Ambulatory w/out assist prior to enrollment

Exclusion criteria

* Red flag signs including fevers, unexplained weight loss, personal history of cancer, tuberculosis exposure, history of spinal infection, history of thoracolumbar spine fracture in the past year as assessed by the clinician. * Use of assistive ambulatory device * Pregnancy * Formal physical therapy within the past 6 months * Neurologic symptoms including weakness or sensory changes in the bilateral lower extremities as assessed by the clinician. * Pain radiating below the posterior pelvic region into either lower extremity * Unwilling or unable to commit to study procedures * Physically incapable of completing PT exercises safely as determined by clinician

Design outcomes

Primary

MeasureTime frameDescription
Scoring of each individual exercise rated by a panel of physiotherapists7 daysA panel of 5 physiotherapists each rates every repetition recorded as acceptable or not. If greater than 90% are rated as acceptable, the exercise will be assessed as acceptable.

Secondary

MeasureTime frameDescription
Rating of exercise execution concerning specific body regions by physiotherapists7 daysFor predefined segments for every exercise, a panel of physiotherapists scores execution quality on a scale of 0-3

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026